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    NDC 64616-0090-02 Fem Repair Non-Preg 14; 6; 6; 6; 7; 15; 6; 12; 10; 20; 6; 20; 6; 6; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL Details

    Fem Repair Non-Preg 14; 6; 6; 6; 7; 15; 6; 12; 10; 20; 6; 20; 6; 6; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL

    Fem Repair Non-Preg is a ORAL LIQUID in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Vitality Works, Inc.. The primary component is ANTIMONY ARSENATE; CENTELLA ASIATICA; CHIONANTHUS VIRGINICUS BARK; CHRYSOPOGON ZIZANIOIDES ROOT; CLAVICEPS PURPUREA SCLEROTIUM; DAPHNE MEZEREUM BARK; GENTIANA LUTEA ROOT; MERCURIUS SOLUBILIS; OXALIC ACID DIHYDRATE; POTASSIUM PHOSPHATE, DIBASIC; RUTA GRAVE.

    Product Information

    NDC 64616-0090
    Product ID 64616-090_0d9b8bfc-62d7-3e8f-e063-6294a90a373b
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Fem Repair Non-Preg
    Proprietary Name Suffix n/a
    Non-Proprietary Name Fem Glandular and Tissue Aid
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 14; 6; 6; 6; 7; 15; 6; 12; 10; 20; 6; 20; 6; 6; 15
    Active Ingredient Units [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
    Substance Name ANTIMONY ARSENATE; CENTELLA ASIATICA; CHIONANTHUS VIRGINICUS BARK; CHRYSOPOGON ZIZANIOIDES ROOT; CLAVICEPS PURPUREA SCLEROTIUM; DAPHNE MEZEREUM BARK; GENTIANA LUTEA ROOT; MERCURIUS SOLUBILIS; OXALIC ACID DIHYDRATE; POTASSIUM PHOSPHATE, DIBASIC; RUTA GRAVE
    Labeler Name Vitality Works, Inc.
    Pharmaceutical Class Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 64616-0090-02 (64616009002)

    NDC Package Code 64616-090-02
    Billing NDC 64616009002
    Package 59 mL in 1 BOTTLE, DROPPER (64616-090-02)
    Marketing Start Date 2013-04-08
    NDC Exclude Flag N
    Pricing Information N/A
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